MDL-1 LASERTRIPTER(TM)— 510(k) K885255
Substantially EquivalentCandela Laser Corp.
FDA 510(k) clearance K885255 for MDL-1 LASERTRIPTER(TM), Substantially Equivalent on 1989-06-01. Applicant: Candela Laser Corp.. Device class: 2.
Clearance details
- Applicant
- Candela Laser Corp.
- Product code
- Code FFK
- Device class
- Class 2
- Regulation
- 21 CFR 876.4480
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wayland, MA, US
Recent devices under product code FFK
view allMore clearances from Candela Laser Corp.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.